Beyond the Extra Respiration of Phagocytosis: NADPH Oxidase 2 in Adaptive Immunity and Inflammation

Front Immunol. 2021 Sep 1:12:733918. doi: 10.3389/fimmu.2021.733918. eCollection 2021.

Abstract

Reactive oxygen species (ROS) derived from the phagocyte NADPH oxidase (NOX2) are essential for host defence and immunoregulation. Their levels must be tightly controlled. ROS are required to prevent infection and are used in signalling to regulate several processes that are essential for normal immunity. A lack of ROS then leads to immunodeficiency and autoinflammation. However, excess ROS are also deleterious, damaging tissues by causing oxidative stress. In this review, we focus on two particular aspects of ROS biology: (i) the emerging understanding that NOX2-derived ROS play a pivotal role in the development and maintenance of adaptive immunity and (ii) the effects of excess ROS in systemic disease and how limiting ROS might represent a therapeutic avenue in limiting excess inflammation.

Keywords: CGD; NOX2; ROS; oxidative stress; systemic inflammation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adaptive Immunity
  • Animals
  • Autoimmunity
  • Cell Respiration
  • Humans
  • Inflammation / immunology*
  • NADPH Oxidase 2 / immunology
  • NADPH Oxidase 2 / metabolism*
  • Oxidative Stress
  • Phagocytosis
  • Reactive Oxygen Species / metabolism

Substances

  • Reactive Oxygen Species
  • NADPH Oxidase 2